A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668533



Internal ID9934638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78677571..78683577hg38UCSC Ensembl
Outerchr11:78677200..78683947hg38UCSC Ensembl
Innerchr11:78388616..78394622hg19UCSC Ensembl
Outerchr11:78388245..78394992hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg386748
hg196748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6529301, essv6311685, essv5912037, essv5866995, essv6594382, essv5962932, essv5570631, essv6202962, essv6476718, essv6516232, essv5694517, essv6007984, essv6571241, essv6162687, essv6566625, essv6161253, essv5831663, essv5961841, essv5645028, essv5715181, essv5718339, essv5686948, essv5946997, essv6143596, essv5686560, essv5525288, essv6120079, essv6311867, essv5916664, essv5805665, essv5854439, essv6330549, essv6083850, essv6169952, essv5973622, essv6442845, essv5884300, essv6273704, essv5610027, essv5433578, essv6199902, essv6138047, essv5898129, essv5436754, essv5781246, essv6268929, essv5717260, essv6455117, essv5867126, essv5868981, essv5961551, essv5829706, essv5650175, essv6579297, essv5992957, essv5456234, essv6287663, essv6305693, essv5920223, essv6335170, essv6590112, essv6536977, essv6157509, essv6390020, essv6155357, essv6549017, essv6536395, essv6363725, essv5608506, essv6591705, essv5763471, essv6122798, essv6291694, essv5520975, essv6302014, essv5625019, essv6336013, essv5473949, essv6202348, essv6430908, essv6351991, essv6215338, essv5680402, essv6560902, essv5490442, essv5503636, essv5810211, essv5837316, essv5558876, essv6188334, essv5617343
SamplesHG01060, HG01441, HG01173, HG01359, HG01052, HG01079, HG01389, HG01374, HG00315, HG00318, HG00181, HG01461, HG01051, HG01140, HG00337, HG00327, HG00271, HG00641, HG01350, HG01070, HG01351, HG00736, HG00346, HG01354, HG01083, HG01365, HG00334, HG00281, HG00277, HG01069, HG01080, HG01067, HG00335, HG00325, HG01072, HG01440, HG00309, HG00338, HG01048, HG00326, HG00323, HG01124, HG01353, HG00313, HG00731, HG00268, HG00282, HG00328, HG00732, HG01095, HG00320, HG00344, HG00275, HG01390, HG01047, HG01102, HG00324, HG00284, HG01073, HG00273, HG01197, HG00331, HG01383, HG01101, HG00321, HG00276, HG01107, HG01075, HG01148, HG00336, HG00285, HG00353, HG00375, HG00278, HG01174, HG01137, HG00319, HG01489, HG01342, HG00339, HG01491, HG00329, HG00342, HG00310, HG00280, HG00343, HG00274, HG01082, HG00345, HG01437, HG01061
Known GenesTENM4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668533
Frequency
Sample Size1151
Observed Gain0
Observed Loss91
Observed Complex0
Frequencyn/a


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